Product Details

SNP ID
rs6918439
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30984001 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAATGTTCTCCTTATGTTTGGTCTA[C/T]TATTGCATTTAGAAGCTGGTGAGTG
Phenotype
MIM: 616991
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MUC21 PubMed Links

Gene Details

Gene
MUC21
Gene Name
mucin 21, cell surface associated
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010909.3 270 Silent Mutation CTA,TTA L15L NP_001010909.2
NM_001322370.1 270 Silent Mutation NP_001309299.1
NM_001322371.1 270 Silent Mutation NP_001309300.1

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